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bn:03519333n
Noun Concept
Categories: Glycoprotein metabolism disorders, Rare diseases, Autosomal recessive disorders
EN
aspartylglucosaminuria  Aga Deficiency  AGU  ASPARTYLGLUCOSAMINIDASE DEFICIENCY  ASPARTYLGLUCOSAMINURIA; AGU
EN
Aspartylglucosaminuria is an inherited disease that is characterized by a decline in mental functioning, accompanied by an increase in skin, bone and joint issues. Wikipedia
Definitions
Relations
Sources
EN
Aspartylglucosaminuria is an inherited disease that is characterized by a decline in mental functioning, accompanied by an increase in skin, bone and joint issues. Wikipedia
A rare genetic illness Wikipedia Disambiguation
Human disease Wikidata
A rare autosomal-recessive lysosomal storage disorder caused by deficient activity of the enzyme aspartylglucosaminidase. Wiktionary
Disorder. Wiktionary (translation)
IS A
rare disease
genetic disease
lysosomal storage disease
neurometabolic disease
GENETIC ASSOCIATION
AGA
HEALTH SPECIALTY
endocrinology
medical genetics
Wikipedia
EN
aspartylglucosaminuria
Wikidata
EN
aspartylglucosaminuria
Wiktionary
EN
aspartylglucosaminuria
Wikipedia Redirections
EN
aspartylglycosaminuria
Wikidata Alias
EN
Aga Deficiency, AGU, ASPARTYLGLUCOSAMINIDASE DEFICIENCY, ASPARTYLGLUCOSAMINURIA, ASPARTYLGLUCOSAMINURIA; AGU, aspartylglycosaminuria, Glycoasparaginase, GLYCOSYLASPARAGINASE DEFICIENCY

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